Variant #0000683965 (NC_000016.9:g.2133674A>G, NC_000016.9(NM_000548.3):c.3884-22A>G (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2133674A>G
DNA change (hg38) g.2083673A>G
Published as -
ISCN -
DB-ID TSC2_001613 See all 2 reported entries
Variant remarks variant in alternatively spliced exon
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site AciI+, BbvI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-08-26 09:13:20 +02:00 (CEST)
Date last edited 2021-08-18 14:45:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -?/-? 32i c.3884-22A>G r.(?) p.(=) - predicted to destroy a branch point


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